Issue |
Europhys. Lett.
Volume 57, Number 4, February 2002
|
|
---|---|---|
Page(s) | 533 - 539 | |
Section | Condensed matter: structure, mechanical and thermal properties | |
DOI | https://doi.org/10.1209/epl/i2002-00494-8 | |
Published online | 01 September 2002 |
Polymer transport across isotope-selective interdiffusion barriers
1
Material Science and Engineering Laboratory, National Institute of Standards and
Technology (NIST) - Gaithersburg, MD 20899-8542, USA
2
Philips Research Laboratories - 5656 AA Eindhoven, The Netherlands
3
Virginia Polytechnic Institute and State University, Department of Chemistry
Blacksburg, VA 24061, USA
Corresponding authors: holger.gruell@philips.com aesker@vt.edu
Received:
26
February
2001
Accepted:
19
November
2001
Neutron reflectivity experiments were performed to study the interdiffusion of two compatible polymers, polystyrene and deuterated polystyrene, across a free-standing ultra-thin (60 Å) interstitial membrane. Annealing above the glass transition temperature and quenching back to room temperature allows for a time-dependent study of the changing concentration profile due to membrane-mediated interdiffusion. For the case of matched polymer molecular masses but different isotopic labeling, faster transport of the deuterated polymer across the interstitial layer is observed leading to displacement of the membrane. Varying the molecular mass and isotopic labeling of the top polymer layer provides information about the size discrimination and isotopic selectivity of the membrane.
PACS: 66.30.Ny – Chemical interdiffusion; diffusion barriers / 68.35.Fx – Diffusion; interface formation / 68.47.Pe – Langmuir-Blodgett films on solids, polymers on surfaces, biological molecules on surfaces
© EDP Sciences, 2002
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